Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs139761834
rs139761834
CD36
3 7 80545045 intron variant T/C snv 2.8E-04 0.700 1.000 1 2018 2018
dbSNP: rs144430312
rs144430312
STAM
1 10 17693720 intron variant T/C snv 3.4E-04 0.700 1.000 1 2018 2018
dbSNP: rs1818782
rs1818782
C9 ; DAB2
3 5 39424526 intron variant A/C snv 0.56 0.700 1.000 1 2018 2018
dbSNP: rs182700961
rs182700961
C2orf16
1 2 27558905 intron variant G/A snv 0.23 0.700 1.000 1 2018 2018
dbSNP: rs2241339
rs2241339
ABCB11
3 2 169013785 intron variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs2489201
rs2489201
CACNB2
1 10 18221519 intron variant G/A snv 0.62 0.700 1.000 1 2018 2018
dbSNP: rs2491441
rs2491441
RGL1
1 1 183833125 intron variant T/C snv 0.16 0.700 1.000 1 2018 2018
dbSNP: rs2804414
rs2804414 		1 10 99761184 TF binding site variant G/A snv 9.0E-02 0.700 1.000 1 2018 2018
dbSNP: rs333947
rs333947
CSF1
7 1 109928142 intron variant G/A snv 0.13 0.700 1.000 1 2018 2018
dbSNP: rs34010237
rs34010237
FCGRT
3 19 49509317 intron variant G/A snv 0.13 0.700 1.000 1 2018 2018
dbSNP: rs4598207
rs4598207 		2 7 50218883 intron variant A/T snv 0.34 0.700 1.000 1 2018 2018
dbSNP: rs4835265
rs4835265
ZNF827
6 4 145900258 intron variant C/A snv 0.15 0.700 1.000 1 2018 2018
dbSNP: rs628401
rs628401 		1 5 73099362 intergenic variant G/A snv 0.46 0.700 1.000 1 2018 2018
dbSNP: rs7043196
rs7043196
AKNA
1 9 114371911 intron variant C/T snv 0.43 0.700 1.000 1 2018 2018
dbSNP: rs72838936
rs72838936
HPSE2
1 10 98480617 intron variant C/T snv 9.4E-02 0.700 1.000 1 2018 2018
dbSNP: rs73550818
rs73550818
GOT2
1 16 58730951 intron variant C/A snv 0.12 0.700 1.000 1 2018 2018
dbSNP: rs738408
rs738408
PNPLA3
10 0.925 0.120 22 43928850 synonymous variant C/T snv 0.28 0.22 0.700 1.000 1 2018 2018
dbSNP: rs74913549
rs74913549
PANX1
3 11 94180526 intron variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs75759936
rs75759936 		3 4 78698045 intergenic variant C/A snv 5.0E-03 0.700 1.000 1 2018 2018
dbSNP: rs7865362
rs7865362
B4GALT1
1 9 33117967 intron variant C/T snv 0.46 0.700 1.000 1 2018 2018
dbSNP: rs79105258
rs79105258
CUX2
24 12 111280427 intron variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs9389268
rs9389268
HBS1L
6 1.000 0.080 6 135098493 intron variant A/G snv 0.24 0.700 1.000 1 2018 2018
dbSNP: rs10272006
rs10272006
SP4
3 0.925 0.080 7 21480514 intron variant G/A snv 0.75 0.700 1.000 1 2019 2019
dbSNP: rs11066280
rs11066280
HECTD4
27 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 0.700 1.000 1 2019 2019
dbSNP: rs117983281
rs117983281
PUM3
1 9 2809077 intron variant C/T snv 1.6E-02 0.700 1.000 1 2019 2019